Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Cds/Sr Cdc

Iqvia
IQVIA
2-5 years
Not Disclosed
Bangalore, India
10 April 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Specialist / Senior Clinical Data Coordinator (CDS / Sr CDC) | Full-Time | Bangalore, India
Experience Required: 2–5 years

Job Description:
We are seeking a detail-oriented Clinical Data Specialist / Senior Clinical Data Coordinator (CDS / Sr CDC) to join our Clinical Data Management (CDM) team in Bangalore. This role focuses on delivering high-quality clinical data management outputs, supporting clinical trials, and ensuring accurate, compliant, and efficient data processes. The position also offers opportunities to take on leadership responsibilities under the guidance of Data Operations leadership.

Key Responsibilities:

  • Provide clinical data management support for assigned studies, ensuring data quality, integrity, and compliance with protocols and SOPs.

  • Serve as a Data Operations Coordinator (DOC) for selected studies or support leadership activities for specific data management functions.

  • Conduct data review and ensure accuracy and completeness of clinical trial data.

  • Create, review, and resolve data queries and clarifications in a timely manner.

  • Assist in database development, testing, and validation, including edit checks and specifications.

  • Perform clinical data coding using standard dictionaries and tools.

  • Support database audits and quality control activities.

  • Act as a backup for Data Operations Coordinator (DOC) or Data Team Lead (DTL) when required.

  • Collaborate with cross-functional teams to maintain efficient study execution and data delivery timelines.

  • Ensure adherence to standard operating procedures, regulatory guidelines, and data management best practices.

Qualifications & Experience:

  • Bachelor’s degree in Life Sciences, Clinical Sciences, Biological Sciences, Mathematics, or a related field.

  • 2–5 years of experience in clinical data management, clinical research, or related roles in CRO or pharmaceutical environments.

  • Exposure to medical terminology and clinical trial processes.

  • Experience with clinical databases, data review, query management, and coding practices.

  • Strong organizational, analytical, and problem-solving skills.

  • Excellent communication, teamwork, and leadership capabilities.

  • Ability to work independently, manage multiple priorities, and maintain attention to detail.

Location: Bangalore, India

Why Join Us:

  • Work with a global leader in clinical research and healthcare intelligence.

  • Gain exposure to end-to-end clinical data management processes and advanced technologies.

  • Collaborate with experienced professionals in a dynamic and growth-driven environment.

  • Access continuous learning opportunities and career advancement in clinical data sciences.